FDA Adverse Event Injury Summary report: N

1043534-2010-00457

MDR report key: 2183264 · Received July 28, 2011

Report

Report Number
1043534-2010-00457
Event Type
Injury
Date Received
July 28, 2011
Report Date
October 13, 2010
Manufacturer
WRIGHT MEDICAL TECHNOLOGY, INC
PMA / PMN Number
K973524
Adverse Event
Yes
Product Problem
Yes
Report Source
Manufacturer report
Reporter Location
AS
Reporter Occupation
OTHER
Health Professional
N

Patients

Seq Age Sex Outcome Treatment
1 NA Unknown Hospitalization| R